The dot chromosome of Drosophila:: Insights into chromatin states and their change over evolutionary time

被引:41
作者
Riddle, Nicole C. [1 ]
Elgin, Sarah C. R. [1 ]
机构
[1] Washington Univ, Dept Biol, St Louis, MO 63130 USA
关键词
chromatin; chromosome evolution; Drosophila; F element; heterochromatin;
D O I
10.1007/s10577-006-1061-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Historically, chromatin has been subdivided into heterochromatin, transcriptionally inactive regions that remain densely packaged throughout the cell cycle, and euchromatin, transcriptionally active regions that take on a diffuse appearance as the cell enters interphase. The banded portion of the small fourth chromosome (dot chromosome) of Drosophila melanogaster is unusual in exhibiting many characteristics of heterochromatic domains, and at the same time maintaining a gene density typical of euchromatin. Similar to genes embedded in pericentric heterochromatin, many of the dot chromosome genes have adapted to a heterochromatic environment. Little is known about the regulation of these genes and less about their evolution in a chromatin context. Interestingly, most of the genes from the D. melanogaster fourth chromosome remain clustered on a small chromosome throughout the genus Drosophila; yet the dot chromosome appears euchromatic in some species, such as D. virilis. Existing genomic sequence data allow an exploration of the underlying differences in DNA sequence organization between species. Here we review the available data describing the dot chromosome, which derives primarily from D. melanogaster. With its unusual and changing nature, the dot chromosome in the genus Drosophila provides a unique opportunity for the examination of transitions between chromatin states during evolution.
引用
收藏
页码:405 / 416
页数:12
相关论文
共 47 条
[1]  
Ashburner M., 2005, DROSOPHILA LAB HDB
[2]   On the abundance and distribution of transposable elements in the genome of Drosophila melanogaster [J].
Bartolomé, C ;
Maside, X ;
Charlesworth, B .
MOLECULAR BIOLOGY AND EVOLUTION, 2002, 19 (06) :926-937
[3]   Y chromosome of D-pseudoobscura is not homologous to the ancestral Drosophila Y [J].
Carvalho, AB ;
Clark, AG .
SCIENCE, 2005, 307 (5706) :108-110
[4]   Genetic definition and sequence analysis of Arabidopsis centromeres [J].
Copenhaver, GP ;
Nickel, K ;
Kuromori, T ;
Benito, MI ;
Kaul, S ;
Lin, XY ;
Bevan, M ;
Murphy, G ;
Harris, B ;
Parnell, LD ;
McCombie, WR ;
Martienssen, RA ;
Marra, M ;
Preuss, D .
SCIENCE, 1999, 286 (5449) :2468-2474
[5]   Drosophila enhancer of Zeste/ESC complexes have a histone H3 methyltransferase activity that marks chromosomal polycomb sites [J].
Czermin, B ;
Melfi, R ;
McCabe, D ;
Seitz, V ;
Imhof, A ;
Pirrotta, V .
CELL, 2002, 111 (02) :185-196
[6]   The HP1 protein family: getting a grip on chromatin [J].
Eissenberg, JC ;
Elgin, SCR .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2000, 10 (02) :204-210
[7]   Chromosomal distribution of Heterochromatin Protein 1 (HP1) in Drosophila:: a cytological map of euchromatic HP1 binding sites [J].
Fanti, L ;
Berloco, M ;
Piacentini, L ;
Pimpinelli, S .
GENETICA, 2003, 117 (02) :135-147
[8]   The rox1 and rox2 RNAs are essential components of the compensasome, which mediates dosage compensation in Drosophila [J].
Franke, A ;
Baker, BS .
MOLECULAR CELL, 1999, 4 (01) :117-122
[9]   Heterochromatin: new possibilities for the inheritance of structure [J].
Grewal, SIS ;
Elgin, SC .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2002, 12 (02) :178-187
[10]   Analyzing heterochromatin formation using chromosome 4 of Drosophila melanogaster [J].
Haynes, KA ;
Leibovitch, BA ;
Rangwala, SH ;
Craig, C ;
Elgin, SCR .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 2004, 69 :267-272